BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families | British Journal of Cancer
Family D in whom deletion of exon 20 of the BRCA1 gene was detected. a.... | Download Scientific Diagram
Genes | Free Full-Text | The Importance of Extended Analysis Using Current Molecular Genetic Methods Based on the Example of a Cohort of 228 Patients with Hereditary Breast and Ovarian Cancer Syndrome | HTML
Normal lymphocyte development and thymic lymphoma formation in Brca1 exon-11-deficient mice | Oncogene
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Phylogenetic Shadowing of Primate Sequences to Find Functional Regions of the Human Genome | Science
BRCA2 T2722R is a deleterious allele that causes exon skipping. - Abstract - Europe PMC
BRCA2 T2722R Is a Deleterious Allele That Causes Exon Skipping - ScienceDirect
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Report BRCA2 T2722R Is a Deleterious Allele That Causes Exon Skipping
Comprehensive splicing functional analysis of DNA variants of the BRCA2 gene by hybrid minigenes | Breast Cancer Research | Full Text
Transcription of CLDND1 in human brain endothelial cells is regulated by the myeloid zinc finger 1 - Shima - 2021 - Clinical and Experimental Pharmacology and Physiology - Wiley Online Library
Average profiles obtained for sequences of housekeeping (HK) and tissue... | Download Scientific Diagram
New RB1 oncogenic mutations and intronic polymorphisms in Serbian retinoblastoma patients: genetic counseling implications | Journal of Human Genetics
Genes | Free Full-Text | Molecular Strategies for RPGR Gene Therapy | HTML
Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations | Nature Reviews Cancer
The Human Prepro-orexin Gene Regulatory Region That Activates Gene Expression in the Lateral Region and Represses It in the Medial Regions of the Hypothalamus* - Journal of Biological Chemistry
Oligonucleotide microarrays demonstrate the highest frequency of ATM mutations in the mantle cell subtype of lymphoma | PNAS
